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United States · US · US:71335-1187_c93fa349-242e-4268-a6d5-0db5564cc181
Escitalopram
Orange BookUNIISPLATC N06AB10
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeN06AB10
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 9
- ndc11713351187130 TABLET, FILM COATED in 1 BOTTLE (71335-1187-1)
- ndc11713351187228 TABLET, FILM COATED in 1 BOTTLE (71335-1187-2)
- ndc11713351187360 TABLET, FILM COATED in 1 BOTTLE (71335-1187-3)
- ndc11713351187490 TABLET, FILM COATED in 1 BOTTLE (71335-1187-4)
- ndc11713351187510 TABLET, FILM COATED in 1 BOTTLE (71335-1187-5)
- ndc117133511876120 TABLET, FILM COATED in 1 BOTTLE (71335-1187-6)
- ndc1171335118777 TABLET, FILM COATED in 1 BOTTLE (71335-1187-7)
- ndc117133511878180 TABLET, FILM COATED in 1 BOTTLE (71335-1187-8)
- ndc117133511879100 TABLET, FILM COATED in 1 BOTTLE (71335-1187-9)
Annotations
UNII (FDA Substance ID)
5U85DBW7LO
ESCITALOPRAM OXALATE
RxCUI 353108
Orange Book
A078032
ABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "5U85DBW7LO",
"rxcui": "353108",
"inchikey": "KTGRHKOEFSJQNS-BDQAORGHSA-N",
"display_name": "ESCITALOPRAM OXALATE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"43eb9e4f-1a46-46f7-9e9d-43e866963b37": {
"match": "brand_token",
"title": "ESCITALOPRAM TABLET, FILM COATED [BRYANT RANCH PREPACK]",
"spl_version": "104",
"published_date": "2026-06-01"
}
},
"productid": "71335-1187_c93fa349-242e-4268-a6d5-0db5564cc181",
"productndc": "71335-1187",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "078032",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 5MG BASE",
"product_no": "001",
"approval_date": "Aug 28, 2015"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 10MG BASE",
"product_no": "002",
"approval_date": "Aug 28, 2015"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 20MG BASE",
"product_no": "003",
"approval_date": "Aug 28, 2015"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "ESCITALOPRAM OXALATE",
"proprietary_name": "Escitalopram",
"active_ingred_unit": "mg/1",
"application_number": "ANDA078032",
"marketing_category": "ANDA",
"nonproprietary_name": "Escitalopram",
"start_marketing_date": "20160201",
"active_numerator_strength": "10"
}Related drugs
Other records sharing ATC code N06AB10.
- CAACH-ESCITALOPRAMACCORD HEALTHCARE INC
- CAACH-ESCITALOPRAMACCORD HEALTHCARE INC
- PLAciprexBiofarm Sp. z o.o.
- CAACT ESCITALOPRAM ODTTEVA CANADA LIMITED
- CAACT ESCITALOPRAM ODTTEVA CANADA LIMITED
- CAAG-ESCITALOPRAMANGITA PHARMA INC.
- CAAG-ESCITALOPRAMANGITA PHARMA INC.
- CAAG-ESCITALOPRAM TABLETSANGITA PHARMA INC.
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